ClinVar Miner

Submissions for variant NM_003098.3(SNTA1):c.743T>C (p.Phe248Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV004764689 SCV005374300 uncertain significance Long QT syndrome 12 2024-09-22 criteria provided, single submitter clinical testing

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